Scientists seek samples to unlock secrets of rare mitochondrial diseases
NCT ID NCT06474104
First seen Oct 31, 2025 · Last updated May 16, 2026 · Updated 28 times
Summary
This study collects blood and skin samples from 100 people with primary mitochondrial diseases and healthy volunteers aged 3 to 85. Researchers will use these samples to understand how different mitochondrial mutations affect cell function and to identify potential biomarkers. The goal is to support the development of a new therapy called mitochondrial augmentation technology (MAT).
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Sheba Medical Center - Tel Ashomer
RECRUITINGRamat Gan, Israel, 5266202, Israel
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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